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No, it's not terminal in itself, but if the heart and aorta are not monitored properly, then there is a chance of sudden death by aortic dissection (the aorta tearing). So, it is definitely life-threatining. Therefore, someone with Marfan syndrome needs an echocardiogram, MRI, CT scan, or TEE of their entire aorta at least once a year to check for aneurysms and monitor their growth. If the aorta is growing rapidly or the valves are leaking a lot, more frequent monitoring is advised. Taking a medication to lower the blood pressure, like beta blockers. Preventative aortic surgery also extends the life expectancy. With proper monitoring, people with Marfan syndrome have an average lfe expectancy.
What else can I help you with?
What are the chances of getting marfan syndrome?
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan syndrome.
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
Is Down Syndrome the same as Marfan Syndrome?
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
What are other names for Marfan Syndrome?
Marfan Syndrome is also known as Marfan's disease and hereditary connective tissue disorder. In some contexts, it may be referred to as Marfan syndrome type I or simply as a connective tissue disorder. However, the most common and widely recognized name remains Marfan Syndrome.
What can be some symptoms for Marfan's syndrome?
flat feet an sinked chest are some symptomes of marfan syndrome
What effects can marfan syndrome have on a persons life?
They cant exercise as vigorously as someone without Marfan syndrome
Can animals have marfan syndrome?
Marfan syndrome is not naturally found in animals. However, researchers have created mice with Marfan syndrome in laboratories for the purpose of testing medications on them before conducting human trials.
When marfan syndrome was discovered?
Marfan syndrome was first described by Antoine Marfan, a French pediatrician, in 1896. He identified the unique characteristics of the syndrome, including tall stature, long limbs, and heart problems.
What is the etiology of marfan syndrome?
The etiology of marfan syndrome would be the mutations in the protein FBN1 in the gene chromosome 15.
How many people in the world haves marfan syndrome?
1 in every 5,00o to 7,000 people have Marfan syndrome.
